Jobs at Enveda Biosciences

Design, build, and maintain scalable data engineering infrastructure on Databricks and Azure. Implement CI/CD, IaC (Pulumi), monitoring, and automation. Collaborate with data scientists and platform teams, improve security and observability, mentor junior engineers, and maintain documentation and internal tooling.

Lead DMPK, clinical pharmacology, and quantitative pharmacology (PK/PD, modeling & simulation) across discovery and development. Drive clinical pharmacology strategy, design and interpret PK/PD studies, support regulatory submissions (IND/NDA/BLA), represent the company with health authorities, manage CRO and cross-functional collaborations, and provide scientific leadership for advancing small-molecule candidates from nomination through clinical development.

Lead global regulatory strategy for small molecules and combination products across development stages. Oversee interactions with FDA, EMA and other agencies; author and submit INDs, CTAs, briefing books, and response packages. Build and manage a high-performing regulatory team covering strategy, operations, and publishing to enable successful regulatory submissions and program advancement.